ibuprofen

Generic: ibuprofen

Labeler: better living brands, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler better living brands, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
BETTER LIVING BRANDS, LLC

Identifiers & Regulatory

Product NDC 21130-006
Product ID 21130-006_067e9eec-ba56-dc37-e063-6294a90a2df2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2023-06-22

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130006
Hyphenated Format 21130-006

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA091239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (21130-006-01) / 100 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-006-05) / 50 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-006-42) / 24 TABLET in 1 BOTTLE
  • 500 TABLET in 1 BOTTLE (21130-006-53)
source: ndc

Packages (4)

21130-006-01 1 BOTTLE in 1 CARTON (21130-006-01) / 100 TABLET in 1 BOTTLE 21130-006-05 1 BOTTLE in 1 CARTON (21130-006-05) / 50 TABLET in 1 BOTTLE 21130-006-42 1 BOTTLE in 1 CARTON (21130-006-42) / 24 TABLET in 1 BOTTLE 21130-006-53 500 TABLET in 1 BOTTLE (21130-006-53)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "067e9eec-ba56-dc37-e063-6294a90a2df2", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["eb60e636-41fe-49fb-e053-2a95a90a0616"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["BETTER LIVING BRANDS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-006-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "21130-006-01", "marketing_start_date": "20230622"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-006-05)  / 50 TABLET in 1 BOTTLE", "package_ndc": "21130-006-05", "marketing_start_date": "20230909"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-006-42)  / 24 TABLET in 1 BOTTLE", "package_ndc": "21130-006-42", "marketing_start_date": "20230622"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (21130-006-53)", "package_ndc": "21130-006-53", "marketing_start_date": "20230828"}], "brand_name": "Ibuprofen", "product_id": "21130-006_067e9eec-ba56-dc37-e063-6294a90a2df2", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-006", "generic_name": "Ibuprofen", "labeler_name": "BETTER LIVING BRANDS, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20230622", "listing_expiration_date": "20261231"}